Literature DB >> 33202249

Gene- and Species-Specific Hox mRNA Translation by Ribosome Expansion Segments.

Kathrin Leppek1, Kotaro Fujii1, Nick Quade2, Teodorus Theo Susanto1, Daniel Boehringer2, Tea Lenarčič2, Shifeng Xue1, Naomi R Genuth1, Nenad Ban3, Maria Barna4.   

Abstract

Ribosomes have been suggested to directly control gene regulation, but regulatory roles for ribosomal RNA (rRNA) remain largely unexplored. Expansion segments (ESs) consist of multitudes of tentacle-like rRNA structures extending from the core ribosome in eukaryotes. ESs are remarkably variable in sequence and size across eukaryotic evolution with largely unknown functions. In characterizing ribosome binding to a regulatory element within a Homeobox (Hox) 5' UTR, we identify a modular stem-loop within this element that binds to a single ES, ES9S. Engineering chimeric, "humanized" yeast ribosomes for ES9S reveals that an evolutionary change in the sequence of ES9S endows species-specific binding of Hoxa9 mRNA to the ribosome. Genome editing to site-specifically disrupt the Hoxa9-ES9S interaction demonstrates the functional importance for such selective mRNA-rRNA binding in translation control. Together, these studies unravel unexpected gene regulation directly mediated by rRNA and how ribosome evolution drives translation of critical developmental regulators.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ES9S; Hox cluster; RNA structure; RNA-protein interaction; expansion segment; internal initiation; internal ribosome entry site; mRNA translation; ribosomal RNA; ribosome; ribosome engineering; stem-loop; yeast

Mesh:

Substances:

Year:  2020        PMID: 33202249      PMCID: PMC7769145          DOI: 10.1016/j.molcel.2020.10.023

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


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